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首页> 外文期刊>Molecular medicine reports >Expression pattern of HMGB1 and its association with autophagy in acute necrotizing pancreatitis
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Expression pattern of HMGB1 and its association with autophagy in acute necrotizing pancreatitis

机译:HMGB1在急性坏死性胰腺炎中的表达模式及其与自噬的关系

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摘要

High-motility group box protein 1 (HMGB1) has an important role in autophagy; however, its exact role in acute necrotizing pancreatitis (ANP) remains unknown. The present study aimed to investigate the expression pattern of HMGB1 in ANP, and to determine its association with autophagy. Sprague Dawley rats (weight, 350 +/- 30 g, n=48) were randomly divided into control (n=12) and experimental (n=36) groups. Experimental rats were retrogradely injected with 5% sodium taurocholate into the biliopancreatic duct to induce ANP. Control rats received an equal amount of saline. Serum amylase levels were used to determine whether the model had been successfully generated. Autophagosomes in pancreatic acinar cells were observed under electron microscopy. The expression levels of HMGB1 and Beclin 1 were detected in pancreatic tissues by western blotting, quantitative polymerase chain reaction and immunohistochemistry. HMGB1 levels were also determined in the serum and in isolated nuclei. The results demonstrated that autophagy was detected at 3 h post-ANP induction; however, HMGB1 expression remained unaltered during the early stage (0-6 h; P>0.05). HMGB1 expression was significantly increased at 12 h, and was still increasing at 24 h (P<0.05). Notably, HMGB1 was increased in the nuclei compared with in the cytoplasm at 3-6 h. Furthermore, serum HMGB1 levels began to increase at 3 h, and reached the highest levels at 24 h in the ANP group. In conclusion, in an ANP model, HMGB1 was initially increased in the nuclei to initiate autophagy. Subsequently, it moved into the cytoplasm, where it interacted with Beclin 1 to enhance autophagy, and HMGB1 was released into the blood, leading to the deterioration of ANP.
机译:高运动性群盒蛋白1(HMGB1)在自噬中起重要作用。然而,其在急性坏死性胰腺炎(ANP)中的确切作用仍然未知。本研究旨在调查HMGB1在ANP中的表达模式,并确定其与自噬的关系。将Sprague Dawley大鼠(体重350 +/- 30 g,n = 48)随机分为对照组(n = 12)和实验组(n = 36)。实验大鼠向胆胰管逆行注射5%牛磺胆酸钠,以诱导ANP。对照大鼠接受等量的盐水。血清淀粉酶水平用于确定模型是否已成功产生。在电子显微镜下观察到胰腺腺泡细胞中的自噬体。通过Western印迹,定量聚合酶链反应和免疫组化检测胰腺组织中HMGB1和Beclin 1的表达水平。还测定了血清和分离的核中的HMGB1水平。结果表明在ANP诱导后3小时检测到自噬。然而,HMGB1的表达在早期(0-6小时; P> 0.05)保持不变。 HMGB1表达在12 h时显着增加,在24 h时仍在增加(P <0.05)。值得注意的是,与3-6小时的细胞质相比,HMGB1在细胞核中增加。此外,ANP组血清HMGB1水平在3 h开始增加,并在24 h达到最高水平。总之,在ANP模型中,HMGB1最初在细胞核中增加以启动自噬。随后,它进入细胞质,与Beclin 1相互作用以增强自噬作用,HMGB1释放到血液中,导致ANP降解。

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